Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

RENAL BIOPSY TRAY

K-Number: K850438 · 1985-02-26

ApplicantPackaging Technologies, Inc.
Decision Date1985-02-26
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RENAL BIOPSY TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Packaging Technologies, Inc.. It received FDA 510(k) clearance on 1985-02-26 under 510(k) number K850438. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RENAL BIOPSY TRAY?

RENAL BIOPSY TRAY is a medical device that received FDA 510(k) clearance on 1985-02-26. The listed applicant is Packaging Technologies, Inc.. The 510(k) number is K850438.

When did RENAL BIOPSY TRAY receive FDA 510(k) clearance?

RENAL BIOPSY TRAY received FDA 510(k) clearance on 1985-02-26, under 510(k) number K850438.

Who is the listed applicant for RENAL BIOPSY TRAY?

The FDA 510(k) record lists Packaging Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RENAL BIOPSY TRAY?

The FDA product code for RENAL BIOPSY TRAY is KNW.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Packaging Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K881756STERILE SURGEONS GLOVESK863326BONE MARROW TRAYK861041ENHANCEK850544SHAVE PREP TRAYK844613GENERAL PURPOSE INSTRUMENT TRAYS SUTURE REMOVAL TRK844614IV START KIT

View all 13 devices →

Related Devices (Code: KNW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260517Automatic Core Biopsy InstrumentZhejiang Curaway Medical Technology Co., Ltd.K262571EnCor EnCompass™ Breast Biopsy and Tissue Removal SystemBard Peripheral Vascular, Inc.K262792Brevera Biopsy System with CorLumina Imaging Technology (BREVDISP09)Hologic, Inc.K260572Marrow MarxmanMedimetrix, LLCK261196Promisemed VeriEcto Automatic Biopsy NeedlesPromisemed Hangzhou Meditech Co., Ltd.K260365Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Control Module; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Disposable Probe, 8 gauge; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Disposable Targeting Set, 8 gauge; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Foot Switch; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Reusable Tray; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Battery CharDevicor Medical Products, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑